Clinical TrialID 7553

Clinical Study of DMT in Healthy Adults

NCT05573568

Healthy Volunteers

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
7553
Evidence Id
7553
Core Evidence Id
7553
Source Clinical Trial Id
7549
Herb2 Clinical Trial Id
HBCT007549
Nct Id
NCT05573568
Title
Clinical Study of DMT in Healthy Adults
Status
Completed
Phase
Phase 1
Study Result
No
Study Condition
Healthy Volunteers
Study Type
Interventional
Study Design
Allocation: NON_RANDOMIZED|Intervention Model: SEQUENTIAL|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: N,N-Dimethyltryptamine
Intervention Allocation
Non_Randomized
Intervention Model
Sequential
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
27
Outcome Measure
Incidence of Treatment-Emergent Adverse Events as clinical and psychiatry symptoms assessed by qualitative medical/clinical-psychiatry evaluation, Evaluate clinical and psychiatry acute risks after DMT treatments assessed by qualitative medical evaluation after dosing., up to 1 month after dosing|Blood Pressure, Assessed 20 times on each dose via systolic and diastolic blood pressure, up to 2 hours after each dose|Heart rate, Assessed 20 times on each dose, up to 2 hours after each dose|Respiratory rate, Assessed 20 times on each dose, up to 2 hours after each dose|Oxygen saturation, Assessed 20 times on each dose, up to 2 hours after each dose
Sponsor Collaborator
Biomind Labs Inc.|Universidade Federal do Rio Grande do Norte
Funded By
INDUSTRY
Location
Hospital Universitário Onofre Lopes, Natal, Rio Grande Do Norte, 59012300, Brazil
Other Id
BMND01
Start Date
2022-06-01
Primary Completion Date
2022-11-01
Completion Date
2022-11-14
First Posted
2022-10-10
Results First Posted
Last Update Posted
2023-02-15
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05573568
Title Cn
Title En
Clinical Study of DMT in Healthy Adults
Bilingual Status
semi_complete